Topical compositions containing a retinoid of the oil-in-water emulsion type

ABSTRACT

A composition in the form of an oil in water emulsion, preferably without emulsifier, is described. The composition can include, in a physiologically acceptable environment, at least one new retinoid. Also described, is the method of preparing the composition and its use in cosmetics and dermatology.

CROSS-REFERENCE TO EARLIER APPLICATION

This application is a non provisional of U.S. Application No. 61/654,729, filed Jun. 1, 2012, which is hereby expressly incorporated by reference in its entirety.

The invention relates to a composition in the form of emulsion comprising, in a physiologically environment, at least one new retinoid with the general formula (I)

where:

-   -   R₁ is a hydrogen atom, an alkyl radical of 1 to 4 carbon atoms         or a —CF₃ radical;     -   R₂ is a hydrogen atom, an alkyl or alkoxy radical of 1 to 4         carbon atoms or a chlorine atom;     -   R₃ is a hydrogen atom, an alkyl or alkoxy radical of 1 to 10         linear or branched carbon atoms, possibly substituted by a         methoxy group;     -   R₄ is a hydrogen atom or an alkyl radical of 1 to 3 carbon         atoms;     -   R₅ is a hydrogen atom or an alkyl radical of 1 to 3 carbon         atoms;     -   or R₄ and R₅ together form, with the bond —N—C(═Y)—, a ring of         the type pyrrolidine, pyrrolidinone, piperidine or piperidinone;     -   Y denotes two hydrogen atoms or one heteroatom such as oxygen or         sulphur;     -   Ar denotes a cyclo 1,4-phenyl, 2,5-pyridyl, 5,2-pyridyl or         2,5-thiophenyl;     -   X denotes an oxygen atom, possibly substituted by an alkyl or         alkylamine chain or a single C—C bond;     -   A denotes a hydrogen atom or the following formula:

-   -   where         -   Q is an oxygen atom or the bond —NH—;         -   R₆ denotes a hydrogen atom, an alkyl radical of 1 to 6             carbon atoms, a cycloalkyl radical of 3 to 6 carbon atoms, a             —C(O)CH₂ or —C(O)CH₂CH₃ radical;         -   R₇ and R₇′ denote, independently of each other, a hydrogen             atom or a hydroxyl group, on condition that R₇ and R₇′ are             not simultaneously a hydroxyl group;         -   n is equal to 0, 1, 2, 3, 4 or 5;

These compounds, described in patent EP1831149, are potent retinoids modulating the nuclear receptor/receptors of retinoic acid (RAR), more specifically of the gamma subtype of this receptor (RARγ).

The receptors RARs activate the transcription by binding with elements of DNA sequences, called the RAR Element (RARE) response elements, in the form of a heterodimer with the X receptors of the retinoids (called RXRs).

Three subtypes of human RARs have been identified and described: RARα, RARβ and RARγ.

Since the gamma RAR receptors are located in the epidermis it is important for the compounds described in the general formula (I) to be released in this part of the skin to provide clinical efficacy.

The topical application of retinoids may result in irrigation of the skin, dryness and erythema. Numerous articles describe this irritating effect, such as the articles by Stucker & al. Skin Res Technol. 2002 May; 8(2):133-40 or by Thielitz & al. Am J Clin Dermatol. 2008; 9(6):369-81.

To obtain topical preparations for pharmaceutical use containing retinoids, numerous techniques are used, in particular emulsions such as those referred to in the patent EP-826366, which describes emulsions which may contain retinoids, or even patent EP-989846, which describes emulsions containing retinoids and at least one emulsifier.

Emulsifiers are molecules that belong to the chemical family of amphiphilic molecules, which are often irritating. Compositions without emulsifiers are in fact less irritating that those containing them.

The fact that emulsifiers are not used in the compositions containing retinoids would therefore enable eliminating cutaneous irritation due to the presence of this class of molecule.

The prior art describes H/E emulsions with or without emulsifier. We may cite, in particular, U.S. Pat. No. 5,851,538, which describes formulations with or without emulsifier with porous microspheres containing a practically continuous network of pores open to the outside and comprising retinoids.

Nevertheless, although the compounds described by the general formula (I) exhibit interesting chemical and physical stability properties for preparations for pharmaceutical uses, they degrade chemically in a number of their solvents.

There is therefore a need for stable, well tolerated pharmaceutical compositions containing compounds described by general formula (I).

A first object according to the invention relates to a pharmaceutical composition comprising a compound with the general formula (I)

where:

-   -   R₁ is a hydrogen atom, an alkyl radical of 1 to 4 carbon atoms         or a —CF₃ radical;     -   R₂ is a hydrogen atom, an alkyl or alkoxy radical of 1 to 4         carbon atoms or a chlorine atom;     -   R₃ is a hydrogen atom, an alkyl or alkoxy radical of 1 to 10         linear or branched carbon atoms, possibly substituted by a         methoxy group;     -   R₄ is a hydrogen atom or an alkyl radical of 1 to 3 carbon         atoms;     -   R₅ is a hydrogen atom or an alkyl radical of 1 to 3 carbon         atoms;     -   or R₄ and R₅ together form, with the bond —N—C(═Y)—, a ring of         the type pyrrolidine, pyrrolidinone, piperidine or piperidinone;     -   Y denotes two hydrogen atoms or one heteroatom such as oxygen or         sulphur;     -   Ar denotes a 1,4-phenyl, 2,5-pyridyl, 5,2-pyridyl or         2,5-thiophenyl ring;     -   X denotes an oxygen atom, possibly substituted by an alkyl or         alkyamine chain or a single C—C bond;     -   A denotes a hydrogen atom or the following formula:

-   -   where:         -   Q is an oxygen atom or the bond —NH—;         -   R₆ denotes a hydrogen atom, an alkyl radical of 1 to 6             carbon atoms, a cycloalkyl radical of 3 to 6 carbon atoms, a             —C(O)CH₂ or —C(O)CH₂CH₃ radical;         -   R₇ and R₇′ denote, independently of each other, a hydrogen             atom or a hydroxyl group, on condition that R₇ and R₇′ are             not simultaneously a hydroxyl group;         -   n is equal to 0, 1, 2, 3, 4 or 5;             at least one gelling agent of the aqueous phase, at least             one principal solvent of the compound (I) and at least one             co-solvent oil of the compound (I).

A second object according to the invention relates to a pharmaceutical composition such as described above for its use as a medicinal product.

A third object according to the invention relates to a pharmaceutical composition as described above for its use in the treatment of pathologies such as:

1) dermatological complaints associated with a keratinisation disorder relating to cellular differentiation and proliferation, particularly for treating common, comedonic, polymorphic acnes, rosaceas, nodulocystic acnes, conglobata, senile acnes and secondary acnes such as solar, medicamentous or professional acne; 2) keratinisation disorders, in particular ichtyoses, ichtyosiform conditions, lamellar ichtyosis, Darrier's disease, palmoplantar keratodermias, leukoplasias, pityriasis rubra pilaris and leukoplasiform conditions, cutaneous or mucous (oral) lichen; 3) dermatological disorders with an inflammatory immune-allergic component, with or without cellular proliferation disorder, and in particular all forms of psoriasis, whether cutaneous, mucous or ungueal, and even psoriasic rheumatic, or atopical dermatitis and the different forms of eczema; 4) cutaneous disorders due to exposure to UV radiation, as well as to repair or control ageing of the skin, whether photo-induced or chronological, or to reduce pigmentations and actinic keratoses, or all pathologies associated with chronological or actinic ageing, such as xerosis, pigmentations and wrinkles; 5) Any condition associated with benign dermal or epidermal proliferations, whether or not of viral origin, such as common warts, flat warts, molluscum contagiosum and verruciform epidermodysplasia, oral or florid papillomatoses; 6) dermatological complaints such as immune dermatoses such as erythematous lupus, bullous immune diseases and collagenic diseases such as sclerodermia; 7) stigmata of epidermal and/or dermal atrophy induced by local or systemic corticosteroids, or any other form of cutaneous atrophy; 8) scarring complaints, or to prevent or repair stretch marks, or even to promote scarring; 9) any disorder of fungal origin in the cutaneous region, such as tinea pedis and tinea versicolor; 10) pigmentation disorders such as hyperpigmentation, melasma, hypopigmentation or vitiligo; 11) cancerous or pre-cancerous, cutaneous or mucous conditions such as actinic keratoses, Bowen's disease, carcinomas in-situ, keratocanthoma and skin cancers such as basocellular carcinoma (BCC), spinocellular carcinoma (SCC)(and cutaneous lymphomas such as T lymphoma.

A fourth object according to the invention relates to a method for preparing a pharmaceutical composition as described above and comprising the following stages:

-   -   a) solubilisation of the hydrophilic excipients under agitation     -   b) solubilisation under agitation of the retinoid in the         phenoxyethanol     -   c) addition of the lipophilic excipients     -   d) gelification of the aqueous phase by adding the polyacryl         amide polymer     -   e) addition of the oily phase then the silicone oil

A fifth object according to the invention relates to the compositions comprising a compound with general formula (I)

And at least one polyacryl amide gelifier, characterised in that the maximum quantity of active ingredient absorbed in the epidermis 16 hours after application, i.e. between 6 ng/cm² and 19 ng/cm².

A sixth object according to the invention relates to the compositions comprising a compound with general formula (I)

And at least polyacryl amide gelifier, characterised in that the maximum quantity of active ingredient absorbed in the epidermis is obtained between 3 and 10 hours after application.

Preferably between 5 and 7 hours after application.

A more detailed description of the invention is detailed hereafter, in the examples and in the figures

DESCRIPTION OF THE INVENTION

To facilitate a reading of this description reference will be made to general formula (1) and compound A in the remaining text, as described thus:

General formula (I):

where:

-   -   R₁ is a hydrogen atom, an alkyl radical of 1 to 4 carbon atoms         or a —CF₃ radical;     -   R₂ is a hydrogen atom, an alkyl or alkoxy radical of 1 to 4         carbon atoms or a chlorine atom;     -   R₃ is a hydrogen atom, an alkyl or alkoxy radical of 1 to 10         linear or branched carbon atoms, possibly substituted by a         methoxy group;     -   R₄ is a hydrogen atom or an alkyl radical of 1 to 3 carbon         atoms;     -   R₅ is a hydrogen atom or an alkyl radical of 1 to 3 carbon         atoms;     -   or R₄ and R₅ together form, with the bond —N—C(═Y)—, a ring of         the type pyrrolidine, pyrrolidinone, piperidine or piperidinone;     -   Y denotes two hydrogen atoms or one heteroatom such as oxygen or         sulphur;     -   Ar denotes a 1,4-phenyl, 2,5-pyridyl, 5,2-pyridyl or         2,5-thiophenyl ring;     -   X denotes an oxygen atom, possibly substituted by an alkyl or         alkyamine chain or a single C—C bond;     -   A denotes a hydrogen atom or the following formula:

-   -   where         -   Q is an oxygen atom or the bond —NH—;         -   R₆ denotes a hydrogen atom, an alkyl radical of 1 to 6             carbon atoms, a cycloalkyl radical of 3 to 6 carbon atoms, a             —C(O)CH₂ or —C(O)CH₂CH₃ radical;         -   R₇ and R₇′ denote, independently of each other, a hydrogen             atom or a hydroxyl group, on condition that R₇ and R₇′ are             not simultaneously a hydroxyl group;         -   n is equal to 0, 1, 2, 3, 4 or 5;

Compound A: as being 3″-tert-butyl-4′-(2-hydroxy-ethoxy)-4″-pyrrolidin-1-yl-[1,1′;3′,1″]-terphenyl-4-carboxylic acid.

Due to the physico-chemical characteristics of the active ingredient, we have had to face a certain number of constraints in the use of the compounds described by general formula (I). These compounds:

-   -   are soluble in few solvents normally used in the fat phases of         the topical emulsions     -   are chemically degraded in a number of their solvents     -   degrade chemically in the presence of numerous emulsifiers.

A first object according to this invention describes compositions containing at least one compound with general formula (I) in the form of emulsions of the type O/W (Oil in Water) and in which the active ingredient is solubilised in the fat phase.

These emulsions exhibit good physical and chemical stability, a rapid rate of penetration and a high level of penetration in the epidermis and/or the dermis.

In a preferred mode, the composition according to the invention is without emulsifier.

Emulsion is understood to mean a macroscopically homogeneous but microscopically heterogeneous mixture of two immiscible liquid substances that we shall call phases. An O/W (oil in water) emulsion consists of a fat (or oily) phase dispersed in an aqueous phase.

In the invention the compositions contain a quantity of active ingredient described by general formula (I) at concentrations ranging from 0.00001% to 1% w/w, preferably from 0.0001 to 0.1% w/w, and more preferably from 0.001 to 0.1% w/w.

Preferably the active ingredient described by general formula (I) is compound A.

-   -   In the invention the compositions contain at least one aqueous         phase gelifier used alone or in combination:     -   Gelling agent means agent capable of giving a composition the         texture of a polymeric gel compound.     -   Gelling agents may be chosen from the plant polymers, gums,         pectins, cellulose and its derivatives, microbiological origin         polymers such as xanthan gum, gelling and synthetic polymers.     -   By way of non-exhaustive example of gelifiers that may enter         into the compositions, mention may be made of Acrylates/C10-30         Alkyl Acrylate Cross polymer, sold under the name of Pemulen         TR-1 or Pemulen TR-2 by the company Noveon, gelifiers in the         polyacryl amide family, such as the mixture of Sodium         acrylamide/acryloyldimethyltaurate         copolymer/isohexadecane/polysorbate 80, sold under the name of         Simulgel 600PHA by the company SEPPIC, and the mixture of         polyacrylamide/isoparaffine C13-14/laureth-7 sold under the name         of Sepigel 305 by the company SEPPIC,     -   The carbomers sold under the name of Ultrez 20®, Ultrez 10®,         Carbopol 1382® or Carbopol ETD2020NF®, Carbopol 981 or even         Carbopol 980 by the company Noveon, the polysaccharides with, by         way of non-exhaustive examples, xanthan gum, such as         Xantura1180® sold by the company Kelco, gellan gum, solder under         the name of Kelcogel by the company Kelco, guar gum, cellulose         and its derivatives, such as microcrystalline cellulose and         carboxymethyl cellulose of sodium sold under the name of Avicel         CL-611 by the company FMC Biopolymer,         hydroxypropylmethylcellulose, in particular the product sold         under the name of Methocel E4M premium by the company Dow         Chemical, or hydroxyethylcellulose, in particular the product         sold under the name of Natrosol HHX 250® by Aqualon, sodium         carboxymethylcellulose, in particular Blanose cellulose gum 7F         sold by the company Aqualon, the family of aluminium magnesium         silicates, such as Veegum K sold by the company Vanderbilt, the         family of acrylic polymers coupled to hydrophobic chains such as         PEG-150/decyl/SMDI copolymer sold under the name of Aculyn 44         (polycondensate, comprising, at least as elements, a         polyethylene glycol with 150 or 180 mols of ethylene oxide,         decyclic alcohol and methylene bis(4-cyclohexylisocyanate)         (SMDI), at 35% by weight in a mixture of propylene glycol (39%)         and water (26%)), the family of modified starches such as         modified potato starch sold under the name of Structure         Solanaceae or their mixtures, the family of the carrageenans,         particularly those distributed among four manor families: κ, λ,         β, ω, such as Viscarin® and the Gelcarin® marketed by the         company IMCD.

In preference a gelifier of the polyacrylamide type, such as Simulgel 600 PHA®, which has thickening and stabilising properties, will be used in concentrations ranging from 0.005 to 5% w/w, and preferably ranging from 1% to 4% w/w, alone or associated with at least one of the above-mentioned gelifiers.

The person skilled in the art knows that for an emulsifier system the proportion of emulsifier required to emulsify a fat phase in an oil in water emulsion is normally of the order of ⅕ of a % of the fat phase. By way of non-exhaustive example a fat phase representing at least 11% of the ingredients of the formulae would require a minimum of 2.5% of emulsifiers.

In the invention, no emulsifier is used as an ingredient in our compositions. However, it is possible that certain ingredients contain low percentages of emulsifier in their own composition. Because of the low percentage that may result from this in our compositions they cannot be used as an emulsifier (lower than 0.6%).

-   -   In the invention the compositions contain a fat phase that may         consist of:         -   a solvent of an active ingredient described by general             formula (I), which may be benzyl alcohol, laureth-4,             phenoxyethanol, propylene glycol monocaprylate, pentylene             glycol or dimethyl isosorbide, and preferably phenoxyethanol             sold under the name phenoxetol by Clariant, the quantity of             phenoxyethanol being 0.2 to 5%, and preferably 0.5 to 2%.         -   one or more co-solvent oils which may be, in preference, the             following co-solvent oils: Caprylic/capric triglycerides             (Miglyol 812N) supplied by IMCD, Prunus Amygdalus Dulcis             (Sweet Almond) oil supplied by SICTIA, Propylene glycol             monocaprylate (Capryol 90) supplied by GATTEFOSSE, Propylene             glycol laurate (Lauroglycol FCC) supplied by GATTEFOSSE,             Sorbitan Sesquioleate (Arlacel 83VPharma) supplied by CRODA,             Diisopropyl Adipate (Crodamol DA) supplied by CRODA, PPG-15             stearyl ether (Arlamol E) supplied by CRODA, Apricot Kernel             Oil PEG-6 Ester (Labrafil M1944CS) supplied by GATTEFOSSE in             proportions ranging from 0.5 to 50% and preferably from 4 to             30%.         -   In the invention the compositions described above may also             contain additives (among which mention may be made of the             following categories, used alone or in combination):         -   Silicon oils that improve the properties of the formula for             the formulation, such as Cyclomethicone (St-Cyclomethicone             5NF) or Dimethicone (Q7 9120 silicon fluid, with a viscosity             of 20 cst to 12500 cst from Dow Corning) between 0 and 10%,             and preferably between 0 and 4%.         -   Preservatives such as methyl parabene, propyl parabene,             benzalconium chloride, phenoxyethanol sold under the name of             phenoxetol by Clariant, benzyl alcohol sold by Merck,             potassium sorbate sold under the name of potassium Sorbate             by VWR, benzoic acid sold under the name Benzoic Acid by             VWR, 2-Bromo-2-Nitropropane-1,3-Diol sold under the name of             Bronopol by Jan Dekker International, Chlorohexidine sold             under the name of Chlorohexidine digluconate 20% solution by             Arnaud Pharmacie, chlorocresol and its derivatives, ethyl             alcohol and diazolidinyl urea. These preservatives may be             used alone or in combination for effective protection of             formulae against all bacterial contamination from 0% to 5%,             and preferably from 0.01 to 2%.         -   Ethanol, the quantity of which is between 0 and 30%,             preferably between 0 and 10%.         -   Moistening agents, preferably polyols and preferably             selected from among propylene glycol, glycerine, diglycerine             or sorbitol (Neosorb supplied by ROQUETTE, Parteck SI             supplied by Merck, but also Sorbitol USP Powder supplied by             LIPO CHEMICALS), whose quantity ranges from 0 to 40% by             weight relative to the total weight of the composition, and             preferably from 5 to 35%.         -   Chelating agents such as EDTA (ethylene diamine tetraacetic             acid) and its derivatives or salts, dihydroglycerine, citric             and tartaric acids, gluconolactone sold under the name             D-(+)-glucono-delta-lactone by MERCK or mixtures thereof.         -   Antioxidants such as vitamin E and its derivatives, such as             DL alpha tocopherol or tocopherol acetate from Roche;             vitamin C and its derivatives, such as Ascorbyl Palmitate             from Roche, Butylhydroxy toluene sold under the name of             Nipanox BHT by Clariant.         -   Palliatives and/or anti-irritants such as PPG-12/SMDI             copolymer sold by Bertek Pharmaceuticals under the             commercial name of Polyolprepolymer-2, glycyrrhetinic acid             or its derivatives, for example Enoxolone sold by Cognis,             hyaluronic acid as such or in its form of sodium hyaluronate             sold under the commercial name of HYAL. NA PWD PH 15-51-45             by Laserson, allantoin sold under the name of RONACARE             ALLANTOINE by MERCK.         -   Any other additive normally used in the pharmaceutical and             cosmetic fields enabling specific properties to be assigned             to the said preparation.

General Composition for Acne:

The percentages are expressed by weight in relation to the total weight of the composition of the oil in water emulsion type.

-   -   from 0.00001% to 1% and preferably from 0.001 to 0.1% of         compound with the general formula (I)     -   from 0.005 to 10% and preferably from 1 to 5% of gelling agent     -   from 0.2 to 5% and preferably from 0.5 to 2% of solvent of         compound with the general formula (I)     -   from 0.5 to 50% and preferably from 4 to 15% of co-solvent oils         of compound with the general formula (I)     -   from 0 to 20% and preferably from 0 to 5% of mineral oils     -   from 0 to 50% and preferably from 5 to 35% of polyol     -   from 0 to 10% and preferably from 0 to 4% of silicone oil     -   from 0 to 5% and preferably from 0.01 to 2% of preservative         system     -   from 0 to 30% and preferably from 0 to 10% of ethanol     -   from 0 to 15% and preferably from 0.1 to 10% of additives

Compositions Suitable for Ichtyosis, Palmoplantar Hyperkeratosis or Psoriasis:

The percentages are expressed by weight in relation to the total weigh of the composition of the oil in water type.

-   -   From 0.00001% to 1% and preferably from 0.001 to 0.12% of         compound with the general formula (I)     -   from 0.005 to 10% and preferably from 1 to 5% of gelling agent     -   from 0.2 to 5% and preferably from 0.5 to 2% of solvent of         compound with the general formula (I)     -   from 0.5 to 50% and preferably from 10 to 30% of co-solvent oils         of compound with the general formula (I)     -   from 1 to 50% and preferably from 10 to 30% of polyol     -   from 0 to 10% and preferably from 0 to 4% of silicone oil     -   from 0 to 5% and preferably from 0.01 to 2% of preservative         system     -   from 0 to 15% and preferably from 0.1 to 10% of additives

Another object according to the invention relates to a method of preparing a composition described as above and comprising the following stages:

A) Preparation of the aqueous phase Solubilisation of the hydrophilic excipients under agitation, if necessary under heat B) Preparation of the oily phase In a suitable receptacle, solubilisation under agitation, of compound A in Phenoxyethanol, under heat if necessary. Allow to return to ambient temperature and add the lipophilic excipients except the silicone oil (ST-cyclomethicone 5 as an example) when this oil is present in the formula to be achieved. C) Mixing of the two phases. At ambient temperature gelify the aqueous phase by adding Simulgel 600PHA, then add the oily phase then the ST-cyclomethicone 5.

EXAMPLES Example Pre-Formulation

In order to obtain an oil in water emulsion containing a compound with the general formula (I) in the fat phase, pre-formulation studies have been conducted to provide evidence of the excipients allowing good solubilisation as well as good stability of the active ingredient.

(1) List of fat phase excipients in which the maximum solubility has been determined by HPLC:

Excipients Maximum solubility Commercial name INCI name % Benzyl alcohol Benzyl Alcohol 2.388 Brij 30 Laureth-4 2.03 Phenoxetol Phenoxyethanol 1.957 Capryol 90 Propylene glycol monocaprylate 0.802 Hydrolite 5P Pentylene glycol 0.482 Arlasolve DMI Dimethyl Isosorbide 0.400 Crodamol IPM Isopropyl myristate <0.1

The limit, below which the compounds of general formula (1) are considered non-solubilized, is 0.1% by weight.

(2) Stability of compound A in its principal solvents:

These stability studies of compound A in its principal solvents show that compound A degrades chemically in a number of its solvents.

These results have enabled us to select our principal solvent (phenoxyethanol) and our co-solvent oils from among the solvent oils which exhibit good stability results, with the aim of developing W/O emulsions in which compound A is solubilised in the oily phase.

Excipients Commercial COMPOUND A name INCI name % Stability results Miglyol 812N Caprylic/capric triglycerides 0.005%  Stable/Ok 6 Months 40° C. Sweet almond oil Prunus Amygdalus Dulcis (Sweet 0.005%  Stable/Ok 6 Months Almond) Oil 40° C. Capryol 90 Propylene glycol monocaprylate 0.05% Stable/Ok 6 Months 40° C. Arlacel 83V Sorbitan Sesquioleate 0.05% Stable/Ok 6 Months Pharma 40° C. Crodamol DA Diisopropyl Adipate 0.05% Stable/Ok 6 Months 40° C. Lauroglycol FCC Propylene glycol laurate 0.05% Stable/Ok 6 Months 40° C. Arlamol E PPG-15 stearyl ether 0.05% Stable/Ok 6 Months 40° C. Phenoxetol Phenoxyethanol 0.05% Stable/Ok 6 Months 40° C. Labrafil Apricot Kernel Oil PEG-6 Ester 0.05% Stable/Ok 6 Months M1944CS 40° C. Dipropylene Dipropylene glycol 0.05% Unstable Glycol Care Brij 30 Laureth-4 0.05% Unstable Benzyl Alcohol Benzyl Alcohol 0.05% Unstable Eutanol G Octyldodecanol 0.05% Unstable Myritol PC Propylene glycol dicaprylate/ 0.05% Unstable dicaprate Arlasolve DMI Dimethyl Isosorbide 0.05% Unstable Marcol 152 Parrafinum liquidum 0.05% Unstable (3) Stability of compound A in mixtures of excipients (solvent/surfactants) determined by HPLC:

Studies of stability of compound A solubilised in oils (in which it is stable) in the presence of surfactants have been conducted:

Mixture of excipients Commercial COMPOUND A name INCI name % Stability results Simulsol M45/ PEG-8 Stearate/Diisopropyl 0.05% Unstable Crodamol DA Adipate Cremophor EL/ PEG-35 Castor Oil/Apricot 0.05% Unstable Labrafil Kernel Oil PEG-6 Ester M1944CS Tween 80/ Polysorbate-80/PPG-15 stearyl 0.05% Unstable Arlamol E ether Cremophor EL/ PEG-35 Castor Oil/Propylene 0.05% Unstable Lauroglycol glycol laurate FCC Tween 80/ Polysorbate-80/Hexylene  0.2% Unstable Hexylene glycol glycol Cremophor EL/ PEG-35 Castor Oil/Apricot  0.2% Unstable Labrafil Kernel Oil PEG-6 Ester M1944CS Cremophor PEG-40 Hydrogenated Castor  0.2% Unstable RH40/ Oil/Diisopropyl Adipate Crodamol DA Tween 80/ Polysorbate-80/Propylene  0.2% Unstable Lauroglycol glycol laurate FCC Simulsol M45/ PEG-8 Stearate/Diisopropyl  0.2% Unstable Crodamol DA Adipate Arlacel 165/ Glyceryl Stearate 0.05% Unstable Lauroglycol PEG-100 Stearate/Propylene FCC glycol laurate GlucateSS- Methyl Glucose Sesquistearate- 0.05% Unstable Glucamate PEG-20 Methyl Glucose SSE-20/ Sesquistearate/PPG-15 stearyl Arlamol E ether Brij 721/ Steareth-21/PPG-15 stearyl 0.05% Stable/Ok 3 Months Arlamol E ether 40° C. Brij 721/ Steareth-21/Propylene glycol 0.05% Stable/Ok 3 Months Lauroglycol laurate 40° C. FCC Eumulgin B2/ Ceteareth-20/PPG-15 stearyl 0.05% Stable/Ok 3 Months Arlamol E ether 40° C. Arlacel 165/ Glyceryl Stearate 0.05% Stable/Ok 3 Months Arlamol E PEG-100 Stearate/PPG-15 40° C. stearyl ether GlucateSS- Methyl Glucose Sesquistearate- 0.05% Stable/Ok 3 Months Glucamate PEG-20 Methyl Glucose 40° C. SSE-20/ Sesquistearate/Propylene Lauroglycol glycol laurate FCC

The limits fixed for high stability are 95%-105% as a percentage relative to TO.

These studies showed that compound A degrades chemically in the presence of numerous surfactants. Following these results we therefore decided to develop an O/W without emulsifier.

Example 2 Formulations

In the following examples the formulae are characterised at TO. The physical and chemical stability of the formulations is achieved after storage at ambient temperature (TA) and at 40° C. after T+1 Month and/or T+2 Months or T+3 Months or T+6 Months. The equipment and methods used for these characteristics are described below.

Since compound A is defined as 3″-tert-butyl-4′-(2-hydroxy-ethoxy)-4″-pyrrolidin-1-yl-[1,1′;3′,1″]-terphenyl-4-carboxylic acid.

Chemical Dose of Compound A:

-   -   Equipment: HPLC     -   Expression of the results: the titre of the active ingredient is         expressed as a % related to the initial % achieved at T0. The         limits fixed for high stability are 95%-105%.

Macroscopic Observation:

-   -   Macroscopic observation enables the physical integrity of the         products at T0 and after stability to be guaranteed.

Microscopic Observation:

-   -   Microscopic observation enables good solubilisation of compound         A from T0, non-recrystallisation in the course of time, as well         as the size of the globules in the oily phase to be evaluated.     -   Equipment: AXIO ZEISS Microscope         pH:     -   Equipment: METTLER TOLEDO Seven Multi pH meter     -   Method: Measurements carried out at ambient temperature after 24         h stabilisation in an enclosure at 25° C. of all the samples.

Viscosity

-   -   The measurement of the viscosity enables the consistency of the         formulae produced to be evaluated.     -   Equipment: Brookfield RV DVII+Pro     -   Method: Measurements carried out at ambient temperature after 24         h stabilisation in an enclosure at 25° C. of all the samples.         The value is read after 1 minute. The choice of mobile phase and         speed will be described in each composition example. The values         obtained are expressed in centipoises (Cps).

Centrifuging:

-   -   The centrifuging enables the resistance of the formulae to a         mechanical stress to be evaluated.     -   Equipment: Galaxy 14D VWR     -   Method: 30 minutes at 5000 rpm     -   A conforming result means that there is neither separation of         phases nor exudate.

Formula 1

COMMERCIAL NAME INCI NAME % COMPOUND A COMPOUND A 0.010 PROPYLENE GLYCOL Propylene Glycol 30.000 ETHANOL 95-96% Ethanol 5.000 RONACARE ALLANTOIN Allantoln 0.200 SIMULGEL 600 PHA Acrylamide, AMPS Copolymer 3.000 Dispersion 40%/ Isohexadecane/polysorbate 80 MIGLYOL 812 N Medium-Chain Triglycerides 8.000 ST-CYCLOMETHICONE 5-NF Cyclopentasiloxane 2.000 PHENOXETOL Phenoxyethanol 1.000 PURIFIED WATER Purified water QSP 100.000 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Very fine, APPEARANCE homogeneous crystal. Ø < 5 μm: 90% pH 5 VISCOSITY Needle 6, Rate 5. 176 000 cp CENTRIFUGING Conforming STABILITY 1 Month 2 Months 3 Months 6 Months MONITORING Physical pH TA/40° C. 5.28/5.31 5.45/5.81 5.30/5.67 5.23/5.75 stability Viscosity TA 169 000 cP 166 000 cP 175 000 cP 172 000 cP 40° C. 174 000 cP 173 000 cP 165 000 cP 159 000 cP Chemical Dose TA 98.70 100.40 100.30 103.10 stability COMPOUND A 40° C. 99.40 101.30  98.80 104.90 Initial %

Formula 2

COMMERCIAL NAME INCI NAME % COMPOUND A COMPOUND A 0.005 PROPYLENE GLYCOL Propylene Glycol 30.000 ETHANOL 95-96% Ethanol 5.000 RONACARE ALLANTOIN Allantoin 0.200 SIMULGEL 600 PHA Acrylamide, AMPS 3.000 Copolymer Dispersion 40%/Isohexadecane/ polysorbate 80 MIGLYOL 812 N Medium-Chain 8.000 Triglycerides ST-CYCLOMETHICONE 5 Cyclopentasiloxane 2.000 PHENOXETOL Phenoxyethanol 1.000 PURIFIED WATER Purified water QSP 100.000 CHARACTERISATION MACROSCOPIC White, smooth, AT T0 APPEARANCE brilliant cream MICROSCOPIC Absence of crystals. Very APPEARANCE fine, homogeneous emulsion. Ø < 5 μm: 90% pH 5 VISCOSITY 176 000 cP CENTRIFUGING Conforming Chemical Dose TA 100.60 100.20 98.00 100.50 stability COMPOUND 40° C. 99.40 100.40 96.80 96.60 A Initial %

Formula 3

COMMERCIAL NAME INCI NAME % COMPOUND A COMPOUND A 0.010 PROPYLENE GLYCOL Propylene Glycol 30.000 BLANOSE CELLULOSE GUM 7H4F Cellulose Gum 0.800 ETHANOL 95-96% Ethanol 5.000 RONACARE ALLANTOIN Allantoin 0.200 SIMULGEL 600 PHA Acrylamide, AMPS Copolymer 2.000 Dispersion 40%/ Isohexadecane/polysorbate 80 MIGLYOL 812 N Triglycerides Medium-Chain 8.000 ST-CYCLOMETHICONE 5 Cyclopentasiloxane 2.000 PHENOXETOL Phenoxyethanol 1.000 PURIFIED WATER Purified water QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Very fine, APPEARANCE homogeneous emulsion. Ø < 5 μm: 90% pH 6.36 VISCOSITY Needle 6, Rate 10. 57 500 cP CENTRIFUGING NR STABILITY MONITORING 1 Month 2 Months 3 Months 6 Months Physical pH TA/40° C. 6.61/6.31 6.7/6.21 6.48/6.18 6.40/6.08 stability Viscosity TA 64 500 cP 59 800 cP 67 000 cP 64 600 cP 40° C. 59 000 cP 59 000 cP 55 100 cP 57 300 cP Chemical Dose TA 104.00 100.5 100.00 95.00 stability COMPOUND 40° C. 104.8 100.00 99.60 94.70 A Initial %

Formula 4

COMMERCIAL NAME INCI NAME % COMPOUND A COMPOUND A 0.010 PROPANEDIOL-1,2 Propylene Glycol 30.000 ETHANOL 95-96% Ethanol 5.000 RONACARE ALLANTOIN Allantoin 0.200 SIMULGEL 600 PHA Acrylamide, AMPS Copolymer 3.000 Dispersion 40%/ Isohexadecane/polysorbate 80 MIGLYOL 812 N Caprylic/Capric Triglyceride 8.000 LABRAFIL M1944CS Apricot Kernel Oil PEG-6 Ester 2.000 ST-CYCLOMETHICONE 5 Cyclopentasiloxane 2.000 PHENOXETOL Phenoxyethanol 1.000 PURIFIED WATER Purified water QSP 100.000 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Very fine, APPEARANCE homogeneous emulsion. Ø < 5 μm: 90% pH 4.72 VISCOSITY Needle 6, Rate 2.5. 215 000 cP CENTRIFUGING NR STABILITY MONITORING 1 Month 2 Months 3 Months 6 Months Physical pH TA/40° C. NR/5.58 NR/5.47 NR/5.53 NR/NR stability Viscosity TA NR NR NR NR 40° C. 183 000 cP 168 000 cP 158 000 cP NR Chemical Dose TA 1.5 Months: 99.90 99.90 NR stability COMPOUND 40° C. 1.5 Months: 99.00 99.40 NR A Initial %

Formula 5

COMMERCIAL NAME INCI NAME % COMPOUND A COMPOUND A 0.010 PROPANEDIOL-1,2 Propylene Glycol 30.000 ETHANOL 95-96% Ethanol 5.000 RONACARE ALLANTOIN Allantoin 0.200 SIMULGEL 600 PHA Acrylamide, AMPS Copolymer 3.000 Dispersion 40%/ Isohexadecane/polysorbate 80 MIGLYOL 812 N Caprylic/Capric Triglyceride 8.000 ARLAMOL PS15E-LQ (WL) PPG-15 stearyl ether 2.000 ST-CYCLOMETHICONE 5-NF Cyclopentasiloxane 2.000 PHENOXETOL Phenoxyethanol 1.000 PURIFIED WATER Purified water QSP 100.000 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 10 μm: 90% pH 4.64 VISCOSITY Needle 6, Rate 2.5. 314 000 cP CENTRIFUGING NR STABILITY MONITORING 1 Month 2 Months 3 Months 6 Months Physical pH TA/40° C. NR/5.62 NR/5.68 NR/5.65 NR/5.81 stability Viscosity TA NR NR NR NR 40° C. 267 000 cP 268 000 cP 262 000 cP 246 000 cP Chemical Dose TA 1.5 Months: 98.80 100.70 107.00 stability COMPOUND A 40° C. 1.5 Months: 106.00 100.70 107.70 Initial %

Formula 6

COMMERCIAL NAME INCI NAME % COMPOUND A COMPOUND A 0.030 PROPANEDIOL-1,2 Propylene Glycol 30.000 ETHANOL 95-96% Ethanol 5.000 RONACARE ALLANTOIN Allantoin 0.200 SIMULGEL 600 PHA Acrylamide, AMPS Copolymer 3.000 Dispersion 40%/ Isohexadecane/polysorbate 80 ST-CYCLOMETHICONE 5NF Cyclopentasiloxane 2.000 CASTOR OIL SEED PH Ricinus Communis (Castor) 8.000 Seed Oil PHENOXETOL Phenoxyethanol 1.000 PURIFIED WATER Purified water QSP 100.000 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 5 μm: 90% pH 5.67 VISCOSITY Needle 29, Rate 0.5. 1 180 000 cP CENTRIFUGING Conforming STABILITY MONITORING 1 Month 2 Months 3 Months 6 Months Physical pH TA/40° C. 5.66/5.55 5.73/5.82 5.44/5.84 5.44/5.84 stability Viscosity TA 1 160 000 cP 1 080 000 1 080 000 cP 1 080 000 cP 40° C. 1 130 000 cP 1 030 000 1 090 000 cP 1 030 000 cP Chemical Dose TA 99.8 100.0 100.4 100.0 stability COMPOUND A 40° C. 99.6  99.5  99.2  99.5 Initial %

Formula 7

COMMERCIAL NAME INCI NAME % COMPOUND A COMPOUND A 0.030 PROPANEDIOL-1,2 Propylene Glycol 30.000 ETHANOL 95-96% Ethanol 5.000 RONACARE ALLANTOIN Allantoin 0.200 SIMULGEL 600 PHA Acrylamide, AMPS Copolymer 3.000 Dispersion 40%/ Isohexadecane/polysorbate 80 MIGLYOL 812 N Caprylic/Capric Triglyceride 4.000 ARLAMOL PS15E-LQ (WL) PPG-15 stearyl ether 4.000 ST-CYCLOMETHICONE 5-NF Cyclopentasiloxane 2.000 PHENOXETOL Phenoxyethanol 1.000 PURIFIED WATER Purified water QSP 100.000 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Fine APPEARANCE homogeneous emulsion. Ø < 5 μm: 90% pH 5.87 VISCOSITY Needle 29, Rate 5. 139 000 cP CENTRIFUGING Conforming STABILITY MONITORING 1 Month 2 Months 3 Months 6 Months Physical pH TA/40° C. 5.90/5.50 5.71/5.71 5.66/5.90 5.66/5.90 stability Viscosity TA 148 000 cP 132000 cP 134 000 cP 132000 cP 40° C. 142 000 cP 130000 cP 137 000 cP 130000 cP Chemical Dose TA  97.8 109.6 100.7 100.7 stability COMPOUND 40° C. 100.0 110.2 100.6 100.2 A Initial %

Formula 8

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.010 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC/CAPRIC 15.00 TRIGLYCERIDES CASTOR OIL PH RICINUS COMMUNIS (CASTOR) 8.00 SEED OIL ST-CYCLOMETHICONE 5NF Cyclopentasiloxane 2.00 Q7-9120 SILICON FLUID DIMETHICONE 5.00 350 cst RONACARE ALLANTOIN ALLANTOIN 0.200 GLYCERINE 4810 GLYCERINE 20.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, AMPS COPOLYMER 3.00 DISPERSION 40%/ ISOHEXADECANE/polysorbate 80 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø 6 μm pH 4.92 VISCOSITY Needle 6, Rate 0.5 NR CENTRIFUGING Conforming Stability monitoring 1 MONTH 2 MONTHS 3 MONTHS 6 MONTHS Physical pH TA/40° C. 4.92/4.88 NR 4.93/5.22 / stability Viscosity TA 192 · 10⁴ cp NR 182 · 10⁴ cp / 40° C. 187 · 10⁴ cp NR 167 · 10⁴ cp /

Formula 9

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.010 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC//CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE 5NF Cyclopentasiloxane 2.00 RONACARE ALLANTOIN ALLANTOIN 0.200 GLYCERINE 4810 VEGETABLE Glycerine 20.00 SIMULGEL 600 PHA ACRYLAMIDE, AMPS 2.5 COPOLYMER DISPERSION 40%/ ISOHEXADECANE/polysorbate 80 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 7 μm pH 4.79 VISCOSITY Needle 6, Rate 5 187000 cp CENTRIFUGING RAS Stability monitoring 1 MONTH 2 MONTHS 3 MONTHS 6 MONTHS Physical pH TA/40° C. 4.76/4.87 4.92/4.99 4.83/5.08 4.59/5.13 stability Viscosity TA 160000 cp 175000 cp 186000 cp 132000 cP 40° C. 154000 cp 146000 cp 146000 cp 137000 cP

Formula 10

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.030 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC//CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE 5NF Cyclopentasiloxane 2.00 RONACARE ALLANTOIN 0.200 ALLANTOIN GLYCERINE 4810 VEGETABLE Glycerine 20.00 SIMULGEL 600 PHA ACRYLAMIDE, AMPS 2.5 COPOLYMER DISPERSION 40%/ ISOHEXADECANE/polysorbate 80 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 7 μm pH 4.76 VISCOSITY Needle 6, Rate 2.5 381000 cp CENTRIFUGING RAS Stability monitoring 1 MONTH 2 MONTHS 3 MONTHS 6 MONTHS Physical pH TA/40° C. 4.74/4.97 4.88/5.00 4.85/5.16 4.96/5.12 stability Viscosity TA 374000 cp 364000 cp 334000 cp 298000 cP 40° C. 288000 cp 266000 cp 269000 cp 260000 cP

Formula 11

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.04 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC//CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE Cyclopentasiloxane 2.00 5NF RONACARE ALLANTOIN ALLANTOIN 0.200 GLYCERINE 4810 Glycerine 20.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, AMPS COPOLYMER 2.5 DISPERSION 40%/ ISOHEXADECANE/polysorbate 80 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 5 μm pH 4.76 VISCOSITY Needle 6, Rate 2.5 340000 cp CENTRIFUGING RAS Stability monitoring 1 MONTH 2 MONTHS 3 MONTHS 6 MONTHS Physical pH TA/40° C. 4.77/4.90 4.92/5.02 5.20/5.15 / stability Viscosity TA 343000 cp 330000 cp 325000 cp / 40° C. 292000 cp 263000 cp 271000 cp /

Formula 12

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.05 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC//CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE Cyclopentasiloxane 2.00 5NF RONACARE ALLANTOIN 0.200 ALLANTOIN GLYCERINE 4810 Glycerine 20.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, AMPS 2.50 COPOLYMER DISPERSION 40%/ ISOHEXADECANE/polysorbate 80 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream TO T0 APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 6 μm pH 4.92 VISCOSITY Needle 6, Rate 2.5 363000 cp CENTRIFUGING RAS Stability monitoring 1 MONTH 2 MONTHS 3 MONTHS 6 MONTHS Physical pH TA/40° C. 4.93/4.88 4.79/4.93 4.87/5.12 / stability Viscosity TA 334000 cp 356000 cp 346000 cp / 40° C. 298000 cp 282000 cp 275000 cp /

Formula 13

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.01 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC//CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE Cyclopentasiloxane 2.00 5NF RONACARE ALLANTOIN ALLANTOIN 0.200 GLYCERINE 4810 Glycerine 20.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, AMPS COPOLYMER 3.00 DISPERSION 40%/ ISOHEXADECANE/polysorbate 80 BENZYL ALCOHOL BENZYL ALCOHOL 0.40 SORBATE DE POTASSIUM SORBATE 0.10 POTASSIUM PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant cream AT T0 APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 5 μm pH 6.64 VISCOSITY Needle 6, Rate 5 147000 cp CENTRIFUGING RAS Stability monitoring 1 MONTH 2 MONTHS 3 MONTHS 6 MONTHS Physical pH TA/40° C. 6.37/6.36 6.60/6.22 6.40/6.13 / stability Viscosity TA 160000 cp 157000 cp 121000 cp /

Formula 14

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.01 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC//CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE Cyclopentasiloxane 2.00 5NF RONACARE ALLANTOIN ALLANTOIN 0.200 GLYCERINE 4810 Glycerine 20.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, AMPS COPOLYMER 3.00 DISPERSION 40%/ ISOHEXADECANE/polysorbate 80 SODIUM BENZOATE SODIUM BENZOATE 0.20 D-(+)-GLUCONO-DELTA- GLUCONOLACTONE 0.25 LACTONE PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION AT T0 MACROSCOPIC White, smooth, brilliant cream APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 8 μm pH 5.44 VISCOSITY Needle 6, Rate 20 36450 cp CENTRIFUGING RAS Stability monitoring 1 MONTH 2 MONTHS 3 MONTHS 6 MONTHS Physical pH TA/ 4.59/4.58 4.70/4.78 NR NR stability 40° C.

Formula 15

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.01 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC//CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE Cyclopentasiloxane 2.00 5NF RONACARE ALLANTOIN 0.200 ALLANTOIN GLYCERINE 4810 Glycerine 20.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, 3.00 AMPS COPOLYMER DISPERSION 40%/ ISOHEXADECANE/ polysorbate 80 BENZYL ALCOHOL BENZYL ALCOHOL 0.80 POTASSIUM SORBATE POTASSIUM SORBATE 0.20 TITRIPLEX III DISODIUM EDTA 0.10 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant AT T0 APPEARANCE cream MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 6 μm pH 6.34 VISCOSITY Needle 5, Rate 5 67920 cp CENTRIFUGING RAS

Formula 16

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.01 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC//CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE Cyclopentasiloxane 2.00 5NF RONACARE ALLANTOIN 0.200 ALLANTOIN GLYCERINE 4810 Glycerine 20.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, 3.00 AMPS COPOLYMER DISPERSION 40%/ ISOHEXADECANE/ polysorbate 80 BENZOIC ACID BENZOIC ACID 0.20 POTASSIUM SORBATE POTASSIUM SORBATE 0.20 TITRIPLEX III DISODIUM EDTA 0.10 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant AT T0 APPEARANCE cream MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 10 μm pH 5.43 VISCOSITY Needle 5, Rate 5 59520 cp CENTRIFUGING RAS

Formula 17

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.01 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC//CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE Cyclopentasiloxane 2.00 5NF RONACARE ALLANTOIN ALLANTOIN 0.200 GLYCERINE 4810 Glycerine 20.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE,AMPS COPOLYMER 2.5 DISPERSION 40%/ ISOHEXADECANE/polysorbate 80 BENZALCONUM BENZALKONIUM CHLORIDE 0.05 CHLORIDE PURIFIED WATER PURIFIED WATER 5.00 POTASSIUM SORBATE POTASSIUM SORBATE 0.20 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION AT T0 MACROSCOPIC White, smooth, brilliant cream APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 7 μm pH 6.82 VISCOSITY Needle 6, Rate 50 11520 cp CENTRIFUGING RAS STABILITY MONITORING 1 Month 2 Months 3 Months 6 Months Physical pH TA/40° C. 6.60/6.43 6.80/6.34 6.61/6.24 6.54/6.23 stability Viscosity TA 11080 cp 10200 cp 11200 cp 9680 cp 40° C. 11760 cp 11400 cp 10720 cp 9520 cp Chemical Dose TA 98.6 100.3 99.7 99.2 stability COMPOUND A 40° C. 97 98.1 97.4 95.4 initial %

Formula 18

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.04 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC//CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE Cyclopentasiloxane 2.00 5NF RONACARE ALLANTOIN ALLANTOIN 0.20 GLYCERINE 4810 Glycerine 20.00 SIMULGEL 600 PHA ACRYLAMIDE, AMPS COPOLYMER 2.5 DISPERSION 40%/ ISOHEXADECANE/polysorbate 80 BENZALCONIUM BENZALKONIUM CHLORIDE 0.05 CHLORIDE PURIFIED WATER PURIFIED WATER 5.00 SORBATE POTASSIUM SORBATE 0.20 DE POTASSIUM PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION AT T0 MACROSCOPIC White, smooth, brilliant cream APPEARANCE MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. Ø < 7 μm pH 6.80 VISCOSITY Needle 6, Rate 50 10920 cp CENTRIFUGING RAS STABILITY MONITORING 1 Month 2 Months 3 Months 6 Months Physical pH TA/40° C. 6.63/6.37 6.67/6.22 6.62/6.25 6.61/6.28 stability Viscosity TA 13340 cp 10450 cp 10540 cp 10840 cp 40° C. 11040 cp NR 10400 cp  9240 cp Chemical Dose TA 100.2 98.3 99.8 99.4 stability COMPOUND 40° C. 99.9 97.5 99.0 96.8 A initial %

Formula 19

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.01 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC/CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE CYCLOPENTASILOXANE 2.00 5NF RONACARE ALLANTOIN 0.20 ALLANTOIN GLYCERINE 4810 GLYCERIN 10.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, 3.00 AMPS COPOLYMER DISPERSION 40%/ ISOHEXADECANE/ POLYSORBATE 80 GLUCONO-DELTA- GLUCONOLACTONE 0.25 LACTONE SG PROBENZ SP SODIUM BENZOATE 0.20 PROPYLENE GLYCOL PROPYLENE GLYCOL 10.00 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant AT T0 APPEARANCE cream MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion. pH 6.80 VISCOSITY Needle 6, Rate 10 59200 cp CENTRIFUGING RAS

Formula 20

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.01 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC/CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE CYCLOPENTASILOXANE 2.00 5NF RONACARE ALLANTOIN 0.20 ALLANTOIN GLYCERINE 4810 GLYCERIN 13.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, 3.00 AMPS COPOLYMER DISPERSION 40%/ ISOHEXADECANE/ POLYSORBATE 80 GLUCONO-DELTA- GLUCONOLACTONE 0.25 LACTONE SG BENZYL ALCOHOL BENZYL ALCOHOL 1.00 PROBENZ SP SODIUM BENZOATE 0.20 PROPYLENE GLYCOL PROPYLENE GLYCOL 7.00 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant AT T0 APPEARANCE cream MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion pH 4.89 VISCOSITY Needle 29, Rate 20 29650 cp CENTRIFUGING RAS

Formula 21

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.01 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC/CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE CYCLOPENTASILOXANE 2.00 5NF RONACARE ALLANTOIN 0.20 ALLANTOIN GLYCERINE 4810 GLYCERIN 15.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, 3.00 AMPS COPOLYMER DISPERSION 40%/ ISOHEXADECANE/ POLYSORBATE 80 GLUCONO-DELTA- GLUCONOLACTONE 0.25 LACTONE SG ALCOOL BENZYLIQUE BENZYL ALCOHOL 1.00 PROBENZ SP SODIUM BENZOATE 0.20 PROPYLENE GLYCOL PROPYLENE GLYCOL 5.00 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant AT T0 APPEARANCE cream MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion pH 4.82 VISCOSITY Needle 29, Rate 12 48583 cp CENTRIFUGING RAS

Formula 22

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.01 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC/CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE CYCLOPENTASILOXANE 2.00 5NF RONACARE ALLANTOIN 0.20 ALLANTOIN TITRIPLEX III EDTA 0.20 GLYCERINE 4810 GLYCERIN 20.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, 2.50 AMPS COPOLYMER DISPERSION 40%/ ISOHEXADECANE/ POLYSORBATE 80 GLUCONO-DELTA- GLUCONOLACTONE 0.25 LACTONE SG ALCOOL BENZYLIQUE BENZYL ALCOHOL 1.00 PROBENZ SP SODIUM BENZOATE 0.20 PURIFIED WATER PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant AT T0 APPEARANCE cream MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion pH 4.97 VISCOSITY Needle 29, Rate 20 29500 cp CENTRIFUGING RAS

Formula 23

COMPOSITIONS Commercial Name INCI name % COMPOUND A COMPOUND A 0.06 PHENOXETOL PHENOXYETHANOL 1.00 MIGLYOL 812N CAPRYLIC/CAPRIC 8.00 TRIGLYCERIDES ARLAMOL PS15E-LQ PPG-15 STEARYL ETHER 15.00 ST-CYCLOMETHICONE CYCLOPENTASILOXANE 2.00 5NF RONACARE ALLANTOIN 0.20 ALLANTOIN GLYCERINE 4810 GLYCERIN 20.00 VEGETABLE SIMULGEL 600 PHA ACRYLAMIDE, 2.50 AMPS COPOLYMER DISPERSION 40%/ ISOHEXADECANE/ POLYSORBATE 80 CHLORURE DE BENZALKONIUM 0.05 BENZALKONIUM CHLORIDE SORBATE DE POTASSIUM SORBATE 0.20 POTASSIUM EAU PURIFIEE PURIFIED WATER QSP 100.00 CHARACTERISATION MACROSCOPIC White, smooth, brilliant TO T0 APPEARANCE cream MICROSCOPIC Absence of crystals. Fine, APPEARANCE homogeneous emulsion pH 6.64 VISCOSITY Needle 5, Rate 10 32320 cp CENTRIFUGING RAS STABILITY MONITORING 1 Month 2 Months 3 Months 6 Months Physical pH 6.58/6.41 6.44/6.23 NR 6.48/6.17 stability TA/40° C. Viscosity 309000 cp 251000 cp 287000 cp 300000 cp TA Needle 5 Rate 1 Viscosity 320000 cp 374000 cp 324000 cp 317000 cp 40° C. Needle 5 Rate 1

Example 3 Characterisation of the Formulations by Cutaneous Penetration Studies on Human Skin

The cutaneous penetration studies enable the formulations to be characterised and the parameters peculiar to each of the formulations to be demonstrated.

Two types of cutaneous penetration studies were carried out ex vivo on human skin. In these studies compound A corresponds to 3″-tert-butyl-4′-(2-hydroxy-ethoxy)-4″-pyrrolidin-1-yl-[1,1′;3′,1″]-terphenyl-4-carboxylic acid.

The reference gel is described as follows:

Constituents % COMPOUND A 0.01 Propylene Glycol 30.00 Ethanol 95-96% 67.99 Klucel HF Pharma 2.00

“Single Time” Cutaneous Penetration Study:

In this study the Formula is applied for 16 hours to the surface of the skin. After the application COMPOUND A is quantified in the different compartments of the skin: stratum corneum, epidermis, dermis and receiving liquid according to the validated bioanalysis method.

The details of the cutaneous application are given in the table below.

Skin: 3 donors, 2 samples per donor Source Entire abdominal human skin Thickness 0.79-1.22 mm Age 39-64 years. Franz cells 2 cm² Volume of receiving liquid 3 mL Barrier function Evaluated by determination of the Insensitive Loss in Water, acceptable except where contraindicated Formulations A: Reference gel containing 100 μg/g B: Oil in water emulsion with emulsifier, of COMPOUND A containing 100 μg/g of COMPOUND A (Formula 3) Application Application ~2 mg/cm² Quantity of active ingredient applied 142~241 ng/cm² Exposure time 16 h Samples taken Donor compartment lavage Kleenex (enabling the surplus product {close oversize brace} “Excess”/Unabsorbed dose {close oversize brace} Mass balance to be removed) 1^(st) strip Stratum corneum (2-15 strips max) Epidermis {close oversize brace} Total skin {close oversize brace} Total penetration Dermis Receiving Liquid } Absorbed dose

The bioanalysis was conducted by mass spectrometry in tandem by positive electrospray ionisation using a Xevo device (Waters). The limit of quantification for compound A is 1 ng/mL.

The conditions of LC/MS/MS developed enabled up to 0.1% of the doe applied in each of the compartments to be detected (unabsorbed dose, stratum, epidermis, dermis and receiving liquid).

The technical conditions are given in the table below.

LC column Hypersil gold 50 * 2.1 mm (UPLC) Mobile phase Phase A: ACN + 0.1% Formic Acid Phase B: H₂O + 0.1% Formic acid Lavage CAN Needle Lavage ACN/H₂O 50:50 septum Gradient Time (min) flow rate % A % B Curve 1. Initial 0.700 15.0 85.0 0 2. 2.5 0.700 90.0 10.0 6 3. 3.20 0.700 90.0 10.0 6 4. 3.25 0.700 15.0 85.0 6 Temperature of columns MSMS ESI+ MRM (Positive electrospray) detection Canal Reaction Dwell (secs) Voltage (cone) Col. Energy Tr (min) COMPOUND 1: 460.26 > 318.20 0.100 50.0 40.0 1.58 COMPOUND A 1: 464.06 > 372.10 0.100 55.0 40.0 1.58 Deuterated Internal Standard Volume 5 μL Injection Run time 4 minutes

In this type of “single point” study the parameters considered are:

-   -   a. The distribution profile in the different compartments         (qualitative data)     -   b. The penetration in the epidermis+dermis compartment         (numerical data)

FIG. 1

The distribution profile between the different compartments is of the same time for the 2 formulae evaluated: accumulation in the stratum corneum, lower rate of precipitation in the epidermis, and very low penetration in the dermis. Compound A is not detected in the receiving liquid.

Penetration values in the epidermis+dermis compartment:

-   -   The penetration values for the oil in water type emulsion         without emulsifier, containing 100 μg/g (0.01%) of compound A         are between 6.8 ng/cm² and 10.6 ng/cm². The levels of         penetration of compound A after application of the oil in water         type emulsion without emulsifier tend to be higher than those         obtained after application of the reference gel.

Penetration Kinetics Study:

In this type of study the penetration of the active ingredient is quantified in each compartment of the skin after 0.5 h, 1 h, 3 h, 6 h and 24 h of application. The penetration kinetics in each compartment are then determined and characterised.

The details of the cutaneous application are given in the table below:

Skin 3 donors, 2 samples per donor per time, n = 6 Source Abdominal human skin dermatomed from corpse Thickness 500 μm Age Not Indicated Franz cells 1-2 cm² Volume of Receiving Liquid Not Indicated Barrier Function Evaluated by tritiated water Products Reference gel 100 μg/g Oil in water type emulsion without emulsifier 100 μg/g (Formula 1) Formula Application ~2 mg/cm² Quantity of active ingredient Between 100-200 ng/cm² applied Exposure time Up to 24 h Samples taken Exposure time 0.5, 1, 3, 6, 24 h Lavage of donor compartment Kleenex (enabling the surplus {close oversize brace} “Excess”/Unabsorbed dose product to be removed) 1^(st) strip Stratum corneum (2-15 strips max) Mass balance Epidermis {close oversize brace} Total Skin {close oversize brace} Dermis Analyses LC/UV and LC/MS Limit of quantification 1 ng/ml

The quantity of active ingredient in each compartment at each time was determined by LC/UV or by LC/MS. The bioanalysis method was validated so that at least 0.1% of the dose applied in each compartment could be detected.

In this type of study the parameters considered are:

-   -   c. The penetration kinetics profile in the epidermis         (qualitative data)     -   d. The initial rate of penetration in the epidermis     -   e. The maximum quantity that has penetrated the epidermis         a. Penetration kinetics profile in the epidermis:

FIG. 2

The release kinetics of compound A obtained for the oil in water type emulsion without emulsifier exhibit a high initial gradient followed by a ceiling during which the penetration of compound A no longer increases in the course of time. The reference formula (gel) shows the same kinetics with rapid release for the first few hours, after which a plateau is reached.

As seen in Section 1 (“Single time” cutaneous penetration study), these two formulae have different penetration levels at 16 h, and the penetration of compound A in the epidermis after application of the oil in water emulsion without emulsifier tends to be higher than that obtained after application of the reference gel.

Initial rate of the kinetics:

-   -   The initial value of the rate of the kinetics or gradient in the         first 3 hours is 4.2 ng/cm²/h.

Maximum quantity in the epidermis:

-   -   The maximum quantity in the epidermis is 18.7 ng/cm².

Example 4 Tolerance Study

In this study:

-   -   10 subjects received 2 grams of gel (reference gel) applied to         1000 cm² for 4 weeks.

A reference gel is understood to mean a gel described as follows:

Constituents % Compound A 0.01 Propylene Glycol 30.00 Ethanol 95-96% 67.99 Klucel HF Pharma 2.00

-   -   10 subjects received 2 grams of Cream B (oil in water emulsion         without emulsifier-Formula 1) applied to 1000 cm² for 4 weeks.

During the study the investigators had the opportunity of changing the area of application where irritation was excessive.

The results of the study are presented in the table below: The numerical values are the number of patients for whom a change of area was made (value N in the table), and the value in brackets is the percentage corresponding to N.

Development of the percentage of subjects for whom there is no change of area of application

Gel Gel 50 μg/g Cream B 50 μg/g Gel Gel 1000 50 μg/g 2000 100 μg/g 25 μg/g cm² 1000 cm² cm² 1000 cm² 1000 cm² Day 2 N (%) — — — — — Day 4 N (%) 1 (10) — — — — Day 5 N (%) — 1 (10) 2 (20) 1 (10) — Day 6 N (%) 1 (10) — — 1 (10) — Day 7 N (%) — — 2 (20) 1 (10) 1 (10) Day 8 N (%) 1 (10) 1 (10) — 2 (20) 1 (10) Day 9 N (%) 3 (30) 1 (10) 2 (20) 1 (10) — Day 10 N (%) — — 1 (10) 1 (10) 1 (10) Day 11 N (%) 2 (20) 1 (10) — 1 (10) 1 (10) Day 12 N (%) — 1 (10) 1 (10) — 1 (10) Day 13 N (%) — 1 (10) — — — Day 14 N (%) 1 (10) 1 (10) 2 (20) 1 (10) 2 (20) Day 16 N (%) 1 (10) 1 (10) — 1 (10) — Day 18 N (%) — — — — 1 (10) Day 19 N (%) — — — — — Day 24 N (%) — 1 (10) — — 1 (10) No N (%) — 1 (10) — — 1 (10) change in the course of the study

FIG. 3

FIG. 3 shows the percentage of subjects for whom there was no change in the area of application as a function of the day of application.

For example, on day 5, for 90% of the subjects receiving Cream B, there was no need to change the area of application. In other words, 10% of the subjects who received Cream B suffered from an irritation requiring a change of area of application.

It is therefore established that the irritation occurs more quickly in the subjects who received the gel than in the subjects who received Cream B. A marked difference is observed from day 9 onwards. 

1. A pharmaceutical composition comprising: An oily phase comprising at least one compound with general formula (I)

where: R₁ is a hydrogen atom, an alkyl radical of 1 to 4 carbons or a —CF₃ radical; R₂ is a hydrogen atom, an alkyl or alkoxy radical of 1 to 4 carbon atoms or a chlorine atom; R₃ is a hydrogen atom, a linear or branched alkyl or alkoxy radical of 1 to 10 carbon atoms optionally substituted by a methoxy group; R₄ is a hydrogen atom or an alkyl radical of 1 to 3 carbon atoms; R₅ is a hydrogen atom or an alkyl radical of 1 to 3 carbon atoms; or R₄ and R₅ together form, with the —N—C(═Y)— bond, a ring of the pyrrolidine, pyrrolidinone, piperidine or piperidinone ring; Y denotes two hydrogen atoms or a heteroatom; Ar denotes a 1,4-phenyl, 2,5-pyridyl, 5,2-pyridyl or 2,5-thiophenyl ring; X denotes an oxygen atom, optionally substituted by an alkyl or alkylamine chain or a single C—C bond; and A denotes a hydrogen atom or the following formula:

where Q is an oxygen atom or a —NH— bond; R₆ denotes a hydrogen atom, an alkyl radical of 1 to 6 carbon atoms, a cycloalkyl radical of 3 to 6 carbon atoms, a —C(O)CH₂ or —C(O)CH₂CH₃ radical; R₇ and R₇′ denote, independently of each other, a hydrogen atom or a hydroxyl group on condition that R₇ and R₇′ are not at the same time a hydroxyl group; and n is equal to 0, 1, 2, 3, 4 or 5; at least a principal solvent of compound (I) and at least a co-solvent oil of compound (I); and an aqueous phase comprising at least a gelifying agent.
 2. The composition according to claim 1, wherein the compound with general formula (I) is defined so that: R1 is a hydrogen atom, the t-butyl or i-propyl radical; R2 is a hydrogen atom, the t-butyl or i-propyl radical; R3 is a hydrogen atom or the ethyl radical; R4, R5 are independently from each other the methyl or ethyl radical or together form a pyrrolidine ring; and A, as previously defined, where R₆ denotes a hydrogen atom, the i-propyl or t-butyl radical, a cycloalkyl radical of 3 to 6 carbon atoms, a —C(O)CH₂ or —C(O)CH₂CH₃ radical.
 3. The composition according to claim 1, wherein the compound is 3″-tert-butyl-4′-(2-hydroxy-ethoxy)-4″-pyrrolidin-1-yl-[1,1′;3′,1″]-terphenyl-4-carboxylic acid.
 4. The composition according to claim 1, wherein the composition is deprived of an emulsifying agent.
 5. The composition according to claim 1, wherein the gelifying agent is selected from: Acrylates/C10-30 Alkyl Acrylate Crosspolymer sold under the name of Pemulen TR-1 or Pemulen TR-2, gelifiers in the family of polyacrylamides, a mixture polyacrylamide/isoparaffin C13-14/laureth-7 sold under the name of Sepigel 305, carbomers sold under the name of Ultrez 20®, Ultrez 10®, Carbopol 1382® or Carbopol ETD2020NF®, Carbopol 981 or even Carbopol 980, polysaccharides with, by way of non-exhaustive example, xanthan gum, gellan gum sold under the name of Kelcogel, guar gum, cellulose, a family of aluminium magnesium silicates, a family of acrylic polymers linked to hydrophobic chains, a family of modified starches or their mixtures, a family of carrageenans.
 6. The composition according to claim 1, wherein the principal solvent is selected from the group consisting of benzyl alcohol, laureth-4, phenoxyethanol, propylene glycol monocaprylate, pentylene glycol and dimethyl isosorbide.
 7. The composition according to claim 1, wherein the principal solvent is phenoxyethanol.
 8. The composition according to claim 1, wherein the co-solvent oil is selected from the group consisting of Caprylic triglycerides/capric, Sweet almond oil, Propylene glycol monocaprylate, Propylene glycol laurate, Sorbitan Sesquioleate, Diisopropyl Adipate, PPG-15 stearyl ether, and Apricot Kernel Oil PEG-6 Ester.
 9. The composition according to claim 1, wherein the composition also contains one or more additives selected from among: A preservative system selected from the group consisting of methyl parabene, propyl parabene, benzalconium chloride, phenoxyethanol sold under the name of phenoxetol, benzyl alcohol sold under the name of benzyl alcohol, Potassium sorbate sold under the name of potassium sorbate, benzoic acid, 2-bromo-2-nitropropane-1,3-diol sold under the name of Bronopol, Chlorohexidine, Chlorohexidine digluconate, chlorocresole and its derivatives, ethyl alcohol and diazolidinyl urea, Chelating agents or mixtures thereof, Antioxidants, Palliatives and/or anti-irritants.
 10. The composition according to claim 1, wherein the composition can contain a mineral oil.
 11. The composition according to claim 1, wherein the composition can also contain a moistening agent.
 12. The composition according to claim 1, wherein the composition can also contain a silicone oil.
 13. The composition according to claim 1, wherein the composition can also contain ethanol.
 14. The composition according to claim 1, wherein the composition comprises the following ingredients: from 0.00001% to 1% w/w of compound A from 0.005 to 10% w/w of gelifier from the aqueous phase from 0.2 to 5% w/w of solvent from 0.5 to 50% w/w of co-solvent oils from 0 to 20% w/w of mineral oils from 0 to 50% w/w of polyol from 0 to 10% w/w of silicone oil from 0 to 5% w/w of preservative system from 0 to 30% w/w of ethanol from 0 to 15% w/w of additives.
 15. The composition according to claim 1, wherein the composition is a water in oil emulsion.
 16. The composition according to claim 1, wherein the maximum quantity of active ingredient absorbed in the dermis and epidermis 16 hours after application is between 6 ng/cm² and 19 ng/cm².
 17. The composition according to claim 16, wherein the maximum quantity of active ingredient absorbed in the dermis and epidermis 16 hours after application is between 6.8 ng/cm² and 10.6 ng/cm².
 18. The composition according to claim 1, wherein the maximum quantity of active ingredient absorbed in the epidermis is attained between 3 hours and 10 hours after application.
 19. A medicinal product comprising the composition according to claim
 1. 20. A method of treating a pathology, the method comprising treating the pathology with an effective amount of the composition of claim 1, wherein the pathology is selected from the group consisting of: Dermatological complaints associated with a keratinization disorder relating to cellular differentiation and proliferation, optionally for treating common, comedonic, polymorphic acnes, rosaceas, nodulocystic acnes, conglobata, senile acnes and secondary acnes optionally solar, medicamentous or professional acne; Keratinisation disorders, optionally ichtyoses, ichtyosiform conditions, lamellar ichtyosis, Darrier's disease, palmoplantar keratodermias, leukoplasias, pityriasis rubra pilaris and leukoplasiform conditions, cutaneous or mucous (oral) lichen; Dermatological disorders with an inflammatory immune-allergic component, with or without cellular proliferation disorder, and optionally all forms of psoriasis, whether cutaneous, mucous or ungueal, and even psoriasic rheumatic, or atopical dermatitis and the different forms of eczema; Cutaneous disorders due to exposure to UV radiation, as well as to repair or control ageing of the skin, whether photo-induced or chronological, or to reduce pigmentations and actinic keratoses, or all pathologies associated with chronological or actinic ageing, such as xerosis, pigmentations and wrinkles; Any condition associated with benign dermal or epidermal proliferations, whether or not of viral origin, optionally common warts, flat warts, molluscum contagiosum and verruciform epidermodysplasia, oral or florid papillomatoses; Dermatological complaints optionally including immune dermatoses optionally erythematous lupus, bullous immune diseases and collagenic diseases such as sclerodermia; Stigmata of epidermal and/or dermal atrophy induced by local or systemic corticosteroids, or any other form of cutaneous atrophy; Scarring complaints, or to treat or repair stretch marks, or even to promote scarring; Any disorder of fungal origin in the cutaneous region, optionally tinea pedis and tinea versicolor; Pigmentation disorders optionally hyperpigmentation, melasma, hypopigmentation or vitiligo; Cancerous or pre-cancerous, cutaneous or mucous conditions optionally actinic keratoses, Bowen's disease, carcinomas in-situ, keratocanthoma and skin cancers optionally basocellular carcinoma (BCC), spinocellular carcinoma (SCC)(and cutaneous lymphomas such as T lymphoma.
 21. The composition of claim 1, wherein when Y is a heteroatom, the heteroatom is oxygen or sulphur.
 22. The composition of claim 5, wherein the gelifier is a sodium acrylamide/acryloyldimethyltaurate/isohexadecane/polysorbate 80 sold under the name of Simulgel 600 PHA.
 23. The composition of claim 5, wherein the xanthan gum is Xantural 180®.
 24. The composition of claim 5, wherein the cellulose is selected from the group consisting of microcrystalline cellulose and carboxymethylcellulose sold under the name Avicel CL-611, hydroxypropylmethylcellulose optionally sold under the name Methocel E4M premium or hydroxyethylcellulose optionally sold under the name Natrosol HHX 250®, sodium carboxymethylcellulose optionally Blanose cellulose gum 7F.
 25. The composition of claim 5, wherein the aluminium magnesium silicate is Veegum K.
 26. The composition of claim 5, wherein the acrylic polymer is PEG-150/decyl/SMDI copolymer sold under the name Aculyn
 44. 27. The composition of claim 5, wherein the modified starch is a modified potato starch sold under the name Structure Solance.
 28. The composition of claim 5, wherein the carrageenan is among the four major families: κ, λ, β, and ω, and is optionally Viscarin® or Geleurin®.
 29. The composition of claim 9, wherein the chelating agent is EDTA (ethylene diamine tetraacetric acid) and its salts, dihydroglycerine, citric acid, tartaric acid, gluconolactone sold under the name D-(+)-glucono-delta-lactone or mixtures thereof.
 30. The composition of claim 9, wherein the antioxidant is vitamin E.
 31. The composition of claim 30, wherein the vitamin E is DL alpha tocopherol or tocopherol acetate.
 32. The composition of claim 9, wherein the antioxidant is vitamin C.
 33. The composition of claim 32, wherein the vitamin C is Ascorbyl Palmitate or Butylhydroxy toluene sold under the name Nipanox BHT.
 34. The composition of claim 9, wherein the palliative or anti-irrant is PPG-12/SMDI copolymer under the name Polyolprepolymer-2, glycyrrhetinic acid, optionally Enoxolone, hyaluronic acid optionally in the form of sodium hyyaluronate sold under the name HYAL. NA PWD PH 15-51-45, an allantoin sold under the name of RONACARE ALLANTOINE.
 35. The composition of claim 14, wherein the composition comprises from 0.0001% to 0.1% w/w of compound A.
 36. The composition of claim 14, wherein the composition comprises from 0.001% to 0.1% w/w of compound A.
 37. The composition of claim 14, wherein the composition comprises from 1% to 5% w/w of gelifier from the aqueous phase.
 38. The composition of claim 14, wherein the composition comprises from 0.5% to 2% w/w of solvent.
 39. The composition of claim 14, wherein the composition comprises from 4% to 30% w/w of co-solvent oils.
 40. The composition of claim 14, wherein the composition comprises from 0% to 5% w/w of mineral oils.
 41. The composition of claim 14, wherein the composition comprises from 5% to 35% w/w of polyol.
 42. The composition of claim 14, wherein the composition comprises 0% to 4% w/w of silicone oil.
 43. The composition of claim 14, wherein the composition comprises from 0.01% to 2% w/w of preservative system.
 44. The composition of claim 14, wherein the composition comprises from 0% to 10% w/w of ethanol.
 45. The composition of claim 14, wherein the composition comprises from 0.1% to 10% w/w of additives. 